HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triisopropyl borate → 3-Fluoro-4-methoxyphenylboronic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 4-Bromo-2-fluoroanisole | HCID 75378 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | 3-Fluoro-4-methoxyphenylboronic acid | HCID 2782194 | — |
Reaction Steps
The title compound was prepared by reacting 4-bromo-2-fluoroanisole (10 g, 0.049 mol) with n-butyl lithium (23.4 mL of 2.5 M solution in hexane, 0.059 mol) followed by triisopropyl borate (45.2 mL, 36.9 g, 0.196 mol) according to method F to yield 7.1 g (85.2%) of a white solid: MS (ESI) m/z 169 (M−H)−: 1H NMR (DMSO-d6): δ 3.84 (3H, s), 7.10–7.16 (1H, m), 7.51–7.60 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07067524B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-62036d36db1f425bab4572e3c8deb253 |
| Source note | uspto-grants-2006_06 |